chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4149261085149261086CT69GENIChomozygous112880972
4149261145149261146CT52GENIChomozygous112880974
4149261207149261208TG51GENICpossibly homozygous112880976
4149261290149261291GC62GENIChomozygous112880978
4149261302149261303GC64GENIChomozygous112880980
4149261570149261570C70GENIChomozygous128090130
4149262475149262476GT48GENIChomozygous112880982
4149262734149262735TG55GENIChomozygous112880983
4149263191149263192AG52GENIChomozygous112880985
4149263832149263833CG47GENIChomozygous112880986
4149264140149264141TC66GENIChomozygous112880988
4149266163149266163A50GENIChomozygous128090131
4149266190149266191CG47GENIChomozygous112880990
4149266735149266736AT49GENIChomozygous112880992
4149267410149267411A43GENIChomozygous128090132
4149267751149267752AG51GENIChomozygous112880993
4149268403149268404AG39GENIChomozygous112880995
4149268735149268736GA70GENIChomozygous112880997
4149268750149268751GC70GENIChomozygous112880999
4149269079149269080GC54GENIChomozygous112881001
4149269399149269400GA55GENIChomozygous112881003
4149269416149269417CT57GENIChomozygous112881005
4149269863149269864GA44GENIChomozygous112881007
4149269917149269918A38GENIChomozygous128090133
4149270013149270014TC39GENIChomozygous112881009
4149270246149270247AG58GENIChomozygous112881011
4149270298149270299TG70GENIChomozygous112881013
4149270389149270390CT66GENIChomozygous112881015
4149272089149272090AG58GENIChomozygous112881017
4149272209149272210AG60GENIChomozygous112881019
4149272287149272288CT64GENIChomozygous112881020
4149272346149272347CG64GENIChomozygous112881022
4149273082149273083GT61GENIChomozygous112881024
4149273177149273178CT49GENIChomozygous112881025
4149273178149273179CT50GENIChomozygous112881027
4149273247149273248GA58GENIChomozygous112881028